fbpx
Wikipedia

Protist shell

Many protists have protective shells or tests,[2] usually made from silica (glass) or calcium carbonate (chalk). Protists are a diverse group of eukaryote organisms that are not plants, animals, or fungi. They are typically microscopic unicellular organisms that live in water or moist environments.

Size comparison between the relatively large coccolithophore Scyphosphaera apsteinii and the relatively small but ubiquitous coccolithophore Emiliania huxleyi[1]

Protists shells are often tough, mineralised forms that resist degradation, and can survive the death of the protist as a microfossil. Although protists are typically very small, they are ubiquitous. Their numbers are such that their shells play a huge part in the formation of ocean sediments and in the global cycling of elements and nutrients.

The role of protist shells depends on the type of protist. Protists such as diatoms and radiolaria have intricate, glass-like shells made of silica that are hard and protective, and serve as a barrier to prevent water loss. The shells have small pores that allow for gas exchange and nutrient uptake. Coccolithophores and foraminifera also have hard protective shells, but the shells are made of calcium carbonate. These shells can help with buoyancy, allowing the organisms to float in the water column and move around more easily.

In addition to protection and support, protist shells also serve scientists as a means of identification. By examining the characteristics of the shells, different species of protists can be identified and their ecology and evolution can be studied.

Protists edit

Cellular life likely originated as single-celled prokaryotes (including modern bacteria and archaea) and later evolved into more complex eukaryotes. Eukaryotes include organisms such as plants, animals, fungi and "protists". Protists are usually single-celled and microscopic. They can be heterotrophic, meaning they obtain nutrients by consuming other organisms, or autotrophic, meaning they produce their own food through photosynthesis or chemosynthesis, or mixotrophic, meaning they produce their own food through a mixture of those methods.

The term protist came into use historically to refer to a group of biologically similar organisms; however, modern research has shown it to be a paraphyletic group that does not contain all descendants of a common ancestor. As such it does not constitute a clade and is not currently in formal scientific use. Nonetheless, the term continues to be used informally to refer to those eukaryotes that cannot be classified as plants, fungi or animals.

Most protists are too small to be seen with the naked eye. They are highly diverse organisms currently organised into 18 phyla, but are not easy to classify.[3][4] Studies have shown high protist diversity exists in oceans, deep sea-vents and river sediments, suggesting large numbers of eukaryotic microbial communities have yet to be discovered.[5][6] As eukaryotes, protists possess within their cell at least one nucleus, as well as organelles such as mitochondria and Golgi bodies. Many protists are asexual but can reproduce rapidly through mitosis or by fragmentation; others (including foraminifera) may reproduce either sexually or asexually.[7]

In contrast to the cells of bacteria and archaea, the cells of protists and other eukaryotes are highly organised. Plants, animals and fungi are usually multi-celled and are typically macroscopic. Most protists are single-celled and microscopic, but there are exceptions, and some marine protists are neither single-celled nor microscopic, such as seaweed.

Silicon-based shells edit

 
A diatom, enclosed in a silica cell wall

Although silicon is readily available in the form of silicates, very few organisms use it directly. Diatoms, radiolaria, and siliceous sponges use biogenic silica as a structural material for their skeletons. In more advanced plants, the silica phytoliths (opal phytoliths) are rigid microscopic bodies occurring in the cell; some plants, including rice, need silica for their growth.[8][9][10] Silica has been shown to improve plant cell wall strength and structural integrity in some plants.[11]

Diatoms edit

Diatoms form a (disputed) phylum containing about 100,000 recognised species of mainly unicellular algae. Diatoms generate about 20 per cent of the oxygen produced on the planet each year,[12] take in over 6.7 billion metric tons of silicon each year from the waters in which they live,[13] and contribute nearly half of the organic material found in the oceans.

Diatoms are enclosed in protective silica (glass) shells called frustules. The beautifully engineered and intricate structure of many of these frustules is such that they are often referred to as "jewels of the sea".[14] Each frustule is made from two interlocking parts covered with tiny holes through which the diatom exchanges nutrients and wastes.[15] The frustules of dead diatoms drift to the ocean floor where, over millions of years, they can build up as much as half a mile deep.[16]

Diatoms uses silicon in the biogenic silica (BSiO2) form,[17] which is taken up by the silicon transport protein to be predominantly used in constructing these protective cell wall structures.[18] Silicon enters the ocean in a dissolved form such as silicic acid or silicate.[19] Since diatoms are one of the main users of these forms of silicon, they contribute greatly to the concentration of silicon throughout the ocean. Silicon forms a nutrient-like profile in the ocean due to the diatom productivity in shallow depths, which means there is less concentration of silicon in the upper ocean and more concentration of silicon in the deep ocean.[19]

Diatom productivity in the upper ocean contribute to the amount of silicon exported to the lower ocean.[20] When diatom cells are lysed in the upper ocean, their nutrients like, iron, zinc, and silicon, are brought to the lower ocean through a process called marine snow. Marine snow involves the downward transfer of particulate organic matter by vertical mixing of dissolved organic matter.[21] Availability of silicon appears crucial for diatom productivity, and as long as silicic acid is available for diatoms to utilize, the diatoms contribute other important nutrient concentrations in the deep ocean.[22]

In coastal zones, diatoms serve as the major phytoplanktonic organisms and greatly contribute to biogenic silica production. In the open ocean, however, diatoms have a reduced role in global annual silica production. Diatoms in North Atlantic and North Pacific subtropical gyres contribute only about 6% of global annual marine silica production, while the Southern Ocean produces about one-third of the global marine biogenic silica.[23] The Southern Ocean is referred to as having a "biogeochemical divide", since only minuscule amounts of silicon is transported out of this region.[24]

Diatom shapes
 
 
Drawings by Haeckel 1904
Diatoms
Diatoms have a silica shell (frustule) with radial (centric) or bilateral (pennate) symmetry
 
Different diatom frustule shapes and sizes
 
Structure of a centric diatom frustule[26]
Diatoms
 
Diatoms, major components of marine plankton, have silica skeletons called frustules. "The microscopic structures of diatoms help them manipulate light, leading to hopes they could be used in new technologies for light detection, computing or robotics.[27]
 
SEM images of pores in diatom frustules[28]

Diatom frustules have been accumulating for over 100 million years, leaving rich deposits of nano and microstructured silicon oxide in the form of diatomaceous earth around the globe. The evolutionary causes for the generation of nano and microstructured silica by photosynthetic algae are not yet clear. However, in 2018 it was shown that absorption of ultraviolet light by nanostructured silica protects the DNA in the algal cells, and this may be an evolutionary cause for the formation of the glass cages.[28][29]

 
Triparma laevis and a drawing of its silicate shell, scale bar = 1 μm.
 
Exploded drawing of the shell, D = dorsal plate, G = girdle plate, S = shield plate and V = ventral plate.
Triparma laevis belongs to the Bolidophyceae, a sister taxon to the diatoms.[30][31]
External videos
  Diatoms: Tiny factories you can see from space
  How diatoms build their beautiful shells – Journey to the Microcosmos

Radiolarians edit

Radiolarian shapes
 
 
Drawings by Haeckel 1904

Radiolarians are unicellular predatory protists encased in elaborate globular shells usually made of silica and pierced with holes. Their name comes from the Latin for "radius". They catch prey by extending parts of their body through the holes. As with the silica frustules of diatoms, radiolarian shells can sink to the ocean floor when radiolarians die and become preserved as part of the ocean sediment. These remains, as microfossils, provide valuable information about past oceanic conditions.[32]

 
An animation of the diversity of radiolarian shells[33]
Fossil radiolarian
 
X-ray microtomography of Triplococcus acanthicus. This is a microfossil from the Middle Ordovician with four nested spheres. The innermost sphere is highlighted red. Each segment is shown at the same scale.[34]
Turing and radiolarian morphology
 
Shell of a spherical radiolarian
 
Shell micrographs
Computer simulations of Turing patterns on a sphere closely replicate some radiolarian shell patterns[35]
External videos
  Radiolarian geometry
  Ernst Haeckel's radiolarian engravings

Calcium-based shells edit

Coccolithophores edit

Coccolithophores are minute unicellular photosynthetic protists with two flagella for locomotion. Most of them are protected by a shell called a coccosphere. Coccospheres are covered with ornate circular plates or scales called coccoliths. The coccoliths are made from calcium carbonate. The term coccolithophore derives from the Greek for a seed carrying stone, referring to their small size and the coccolith stones they carry. Under the right conditions they bloom, like other phytoplankton, and can turn the ocean milky white.[36]

Coccolithophores
 
Have plates called coccoliths
 
Extinct fossil
Coccolithophores build calcite skeletons important to the marine carbon cycle[37]

There are benefits for protists that carry protective shells. The diagram on the left below shows some benefits coccolithophore get from carrying coccoliths. In the diagram, (A) represents accelerated photosynthesis including carbon concentrating mechanisms (CCM) and enhanced light uptake via scattering of scarce photons for deep-dwelling species. (B) represents protection from photodamage including sunshade protection from ultraviolet light (UV) and photosynthetic active radiation (PAR) and energy dissipation under high-light conditions. (C) represents armour protection includes protection against viral/bacterial infections and grazing by selective and nonselective grazers.[38]

Benefits of having shells
 
Benefits in coccolithophore calcification[38] – see text above
Costs of having shells
 
Energetic costs in coccolithophore calcification[38]

There are also costs for protists that carry protective shells. The diagram on the right above shows some of the energetic costs coccolithophore incur from carrying coccoliths. In the diagram, the energetic costs are reported in percentage of total photosynthetic budget. (A) represents transport processes include the transport into the cell from the surrounding seawater of primary calcification substrates Ca2+ and HCO3− (black arrows) and the removal of the end product H+ from the cell (gray arrow). The transport of Ca2+ through the cytoplasm to the coccolith vesicle (CV) is the dominant cost associated with calcification. (B) represents metabolic processes include the synthesis of coccolith-associated polysaccharides (CAPs – gray rectangles) by the Golgi complex (white rectangles) that regulate the nucleation and geometry of CaCO3 crystals. The completed coccolith (gray plate) is a complex structure of intricately arranged CAPs and CaCO3 crystals. (C) Mechanical and structural processes account for the secretion of the completed coccoliths that are transported from their original position adjacent to the nucleus to the cell periphery, where they are transferred to the surface of the cell.[38]

Foraminiferans edit

Foraminiferan shapes
 
 
Drawings by Haeckel 1904

Like radiolarians, foraminiferans (forams for short) are single-celled predatory protists, also protected with shells that have holes in them. Their name comes from the Latin for "hole bearers". Their shells, often called tests, may be single-chambered or multi-chambered; multi-chambered forams add more chambers as they grow. The most famous of these are made of calcite, but tests may also be made of aragonite, agglutinated sediment particles, chiton, or (rarely) of silica. Most forams are benthic, but about 40 living species are planktic.[39] They are widely researched with well established fossil records which allow scientists to infer a lot about past environments and climates.[32] Some foraminifera lack tests altogether.[40]

Foraminiferans
 
Empty Foraminiferan test, showing multiple chambers and pores
 
...and in life, showing pseudopodia streaming from pores
Foraminiferans are important unicellular zooplankton protists, often with calcite tests
External videos
  foraminiferans
  Foraminiferal networks and growth
 
Benthic foraminifera Favulina hexagona, together with nanofossils enclosed inside the shell hexagons[41]

Other shells edit

 
Testate amoeba

The cell body of many choanoflagellates is surrounded by a distinguishing extracellular matrix or periplast. These cell coverings vary greatly in structure and composition and are used by taxonomists for classification purposes. Many choanoflagellates build complex basket-shaped "houses", called lorica, from several silica strips cemented together.[43] The functional significance of the periplast is unknown, but in sessile organisms, it is thought to aid attachment to the substrate. In planktonic organisms, there is speculation that the periplast increases drag, thereby counteracting the force generated by the flagellum and increasing feeding efficiency.[43][44]

External videos
  Testate amoebas: blobby, modest shell dwellers                         Journey to the Microcosmos

Microfossils and sediments edit

 
Diatomaceous earth is a soft, siliceous, sedimentary rock made up of microfossils in the form of the frustules (shells) of single cell diatoms. This sample consists of a mixture of centric (radially symmetric) and pennate (bilaterally symmetric) diatoms. Click 3 times to fully enlarge.

The shells or skeletons of many protists survive over geological time scales as microfossils. Microfossils are fossils that are generally between 0.001mm and 1 mm in size,[45] the study of which requires the use of light or electron microscopy. Fossils which can be studied by the naked eye or low-powered magnification, such as a hand lens, are referred to as macrofossils.

Microfossils are a common feature of the geological record, from the Precambrian to the Holocene. They are most common in marine sediments, but also occur in brackish water, fresh water and terrestrial sedimentary deposits. While every kingdom of life is represented in the microfossil record, the most abundant forms are protist skeletons or cysts from the Chrysophyta, Pyrrhophyta, Sarcodina, acritarchs and chitinozoans, together with pollen and spores from the vascular plants.

In 2017, fossilized microorganisms, or microfossils, were discovered in hydrothermal vent precipitates in the Nuvvuagittuq Belt that may be as old as 4.28 billion years old, the oldest record of life on Earth, suggesting "an almost instantaneous emergence of life" (in a geological time-scale sense), after ocean formation 4.41 billion years ago, and not long after the formation of the Earth 4.54 billion years ago.[46][47][48][49] Nonetheless, life may have started even earlier, at nearly 4.5 billion years ago, as claimed by some researchers.[50][51]

See also edit

References edit

  1. ^ Gafar, N. A., Eyre, B. D. and Schulz, K. G. (2019) "A comparison of species specific sensitivities to changing light and carbonate chemistry in calcifying marine phytoplankton". Scientific Reports, 9(1): 1–12. doi:10.1038/s41598-019-38661-0.   Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
  2. ^ "Groups of Protists | Boundless Biology". courses.lumenlearning.com. Retrieved 16 February 2021.
  3. ^ Cavalier-Smith T (December 1993). "Kingdom protozoa and its 18 phyla". Microbiological Reviews. 57 (4): 953–94. doi:10.1128/mmbr.57.4.953-994.1993. PMC 372943. PMID 8302218.
  4. ^ Corliss JO (1992). "Should there be a separate code of nomenclature for the protists?". BioSystems. 28 (1–3): 1–14. doi:10.1016/0303-2647(92)90003-H. PMID 1292654.
  5. ^ Slapeta J, Moreira D, López-García P (2005). "The extent of protist diversity: insights from molecular ecology of freshwater eukaryotes". Proceedings of the Royal Society B: Biological Sciences. 272 (1576): 2073–81. doi:10.1098/rspb.2005.3195. PMC 1559898. PMID 16191619.
  6. ^ Moreira D, López-García P (2002). "The molecular ecology of microbial eukaryotes unveils a hidden world" (PDF). Trends in Microbiology. 10 (1): 31–8. doi:10.1016/S0966-842X(01)02257-0. PMID 11755083.
  7. ^ Foraminifera: notes for a short course organized by M.A. Buzas and B.K. Sen Gupta: prepared for the short course on foraminifera sponsored by the Paleontological Society, held at New Orleans, Louisiana, October 17, 1982. Thomas W. Broadhead, Paleontological Society. [Knoxville, Tenn.]: University of Tennessee, Dept. of Geological Sciences. 1982. ISBN 0-910249-05-9. OCLC 9276403.{{cite book}}: CS1 maint: others (link)
  8. ^ Rahman, Atta-ur- (2008). "Silicon". Studies in Natural Products Chemistry. Vol. 35. p. 856. ISBN 978-0-444-53181-0.
  9. ^ Exley, C. (1998). "Silicon in life:A bioinorganic solution to bioorganic essentiality". Journal of Inorganic Biochemistry. 69 (3): 139–144. doi:10.1016/S0162-0134(97)10010-1.
  10. ^ Epstein, Emanuel (1999). "SILICON". Annual Review of Plant Physiology and Plant Molecular Biology. 50: 641–664. doi:10.1146/annurev.arplant.50.1.641. PMID 15012222.
  11. ^ Kim, Sang Gyu; Kim, Ki Woo; Park, Eun Woo; Choi, Doil (2002). "Silicon-Induced Cell Wall Fortification of Rice Leaves: A Possible Cellular Mechanism of Enhanced Host Resistance to Blast". Phytopathology. 92 (10): 1095–103. doi:10.1094/PHYTO.2002.92.10.1095. PMID 18944220.
  12. ^ The Air You're Breathing? A Diatom Made That
  13. ^ Treguer, P.; Nelson, D. M.; Van Bennekom, A. J.; Demaster, D. J.; Leynaert, A.; Queguiner, B. (1995). "The Silica Balance in the World Ocean: A Reestimate". Science. 268 (5209): 375–9. Bibcode:1995Sci...268..375T. doi:10.1126/science.268.5209.375. PMID 17746543. S2CID 5672525.
  14. ^ Ireland, T., "Engineering with algae". Biologist, 63(5): 10.
  15. ^ Wassilieff, Maggy (2006) "Plankton - Plant plankton", Te Ara - the Encyclopedia of New Zealand. Accessed: 2 November 2019.
  16. ^ "King's College London - Lake Megachad". www.kcl.ac.uk. Retrieved 5 May 2018.
  17. ^ Bidle, Kay D.; Manganelli, Maura; Azam, Farooq (6 December 2002). "Regulation of Oceanic Silicon and Carbon Preservation by Temperature Control on Bacteria". Science. 298 (5600): 1980–1984. Bibcode:2002Sci...298.1980B. doi:10.1126/science.1076076. ISSN 0036-8075. PMID 12471255. S2CID 216994.
  18. ^ Durkin, Colleen A.; Koester, Julie A.; Bender, Sara J.; Armbrust, E. Virginia (2016). "The evolution of silicon transporters in diatoms". Journal of Phycology. 52 (5): 716–731. doi:10.1111/jpy.12441. ISSN 1529-8817. PMC 5129515. PMID 27335204.
  19. ^ a b Dugdale, R. C.; Wilkerson, F. P. (30 December 2001). "Sources and fates of silicon in the ocean: the role of diatoms in the climate and glacial cycles". Scientia Marina. 65 (S2): 141–152. doi:10.3989/scimar.2001.65s2141. ISSN 1886-8134.
  20. ^ Baines, Stephen B.; Twining, Benjamin S.; Brzezinski, Mark A.; Krause, Jeffrey W.; Vogt, Stefan; Assael, Dylan; McDaniel, Hannah (December 2012). "Significant silicon accumulation by marine picocyanobacteria". Nature Geoscience. 5 (12): 886–891. Bibcode:2012NatGe...5..886B. doi:10.1038/ngeo1641. ISSN 1752-0908.
  21. ^ Turner, Jefferson T. (January 2015). "Zooplankton fecal pellets, marine snow, phytodetritus and the ocean's biological pump". Progress in Oceanography. 130: 205–248. Bibcode:2015PrOce.130..205T. doi:10.1016/j.pocean.2014.08.005. ISSN 0079-6611.
  22. ^ Yool, Andrew; Tyrrell, Toby (2003). "Role of diatoms in regulating the ocean's silicon cycle". Global Biogeochemical Cycles. 17 (4): n/a. Bibcode:2003GBioC..17.1103Y. doi:10.1029/2002GB002018. ISSN 1944-9224. S2CID 16849373.
  23. ^ Tréguer, Paul J.; De La Rocha, Christina L. (3 January 2013). "The World Ocean Silica Cycle". Annual Review of Marine Science. 5 (1): 477–501. doi:10.1146/annurev-marine-121211-172346. PMID 22809182.
  24. ^ Marinov, I.; Gnanadesikan, A.; Toggweiler, J. R.; Sarmiento, J. L. (June 2006). "The Southern Ocean biogeochemical divide". Nature. 441 (7096): 964–967. Bibcode:2006Natur.441..964M. doi:10.1038/nature04883. PMID 16791191. S2CID 4428683.
  25. ^ Arsenieff, L.; Simon, N.; Rigaut-Jalabert, F.; Le Gall, F.; Chaffron, S.; Corre, E.; Com, E.; Bigeard, E.; Baudoux, A.C. (2018). "First Viruses Infecting the Marine Diatom Guinardia delicatula". Frontiers in Microbiology. 9: 3235. doi:10.3389/fmicb.2018.03235. PMC 6334475. PMID 30687251.
  26. ^ Zhang, D.; Wang, Y.; Cai, J.; Pan, J.; Jiang, X.; Jiang, Y. (2012). "Bio-manufacturing technology based on diatom micro- and nanostructure". Chinese Science Bulletin. 57 (30): 3836–3849. Bibcode:2012ChSBu..57.3836Z. doi:10.1007/s11434-012-5410-x.
  27. ^ Biodegradable glitter and pollution-eating microalgae: the new materials inspired by nature Horizon, 28 May 2020.
  28. ^ a b Aguirre, L. E., Ouyang, L., Elfwing, A., Hedblom, M., Wulff, A. and Inganäs, O. (2018) "Diatom frustules protect DNA from ultraviolet light". Scientific reports, 8(1): 1–6. doi:10.1038/s41598-018-21810-2.   Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
  29. ^ De Tommasi, E., Congestri, R., Dardano, P., De Luca, A.C., Managò, S., Rea, I. and De Stefano, M. (2018) "UV-shielding and wavelength conversion by centric diatom nanopatterned frustules". Scientific Reports, 8(1): 1–14. doi:10.1038/s41598-018-34651-w.   Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
  30. ^ Booth, B.C. and Marchant, H.J. (1987) "Parmales, a new order of marine chrysophytes, with descriptions of three new genera and seven new species". Journal of Phycology, 23: 245–260. doi:10.1111/j.1529-8817.1987.tb04132.x.
  31. ^ Kuwata, A., Yamada, K., Ichinomiya, M., Yoshikawa, S., Tragin, M., Vaulot, D. and Lopes dos Santos, A. (2018) "Bolidophyceae, a sister picoplanktonic group of diatoms – a review". Frontiers in Marine Science, 5: 370. doi:10.3389/fmars.2018.00370.   Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
  32. ^ a b Wassilieff, Maggy (2006) "Plankton - Animal plankton", Te Ara - the Encyclopedia of New Zealand. Accessed: 2 November 2019.
  33. ^ Kachovich, Sarah (2018) "Minds over Methods: Linking microfossils to tectonics" Blog of the Tectonics and Structural Geology Division of the European Geosciences Union.
  34. ^ Kachovich, S., Sheng, J. and Aitchison, J. C., 2019. Adding a new dimension to investigations of early radiolarian evolution. Scientific reports, 9(1), pp. 1–10. doi:10.1038/s41598-019-42771-0.   Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
  35. ^ Varea, C.; Aragon, J. L.; Barrio, R. A. (1999). "Turing patterns on a sphere". Physical Review E. 60 (4): 4588–4592. Bibcode:1999PhRvE..60.4588V. doi:10.1103/PhysRevE.60.4588. PMID 11970318.
  36. ^ Wassilieff, Maggy (2006) "A coccolithophore", Te Ara - the Encyclopedia of New Zealand. Accessed: 2 November 2019.
  37. ^ Rost, B. and Riebesell, U. (2004) "Coccolithophores and the biological pump: responses to environmental changes". In: Coccolithophores: From Molecular Processes to Global Impact, pages 99–125, Springer. ISBN 9783662062784.
  38. ^ a b c d Monteiro, F.M., Bach, L.T., Brownlee, C., Bown, P., Rickaby, R.E., Poulton, A.J., Tyrrell, T., Beaufort, L., Dutkiewicz, S., Gibbs, S. and Gutowska, M.A. (2016) "Why marine phytoplankton calcify". Science Advances, 2(7): e1501822. doi:10.1126/sciadv.1501822.   Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
  39. ^ Hemleben, C.; Anderson, O.R.; Spindler, M. (1989). Modern Planktonic Foraminifera. Springer-Verlag. ISBN 978-3-540-96815-3.
  40. ^ Pawlowski, Jan; Bolivar, Ignacio; Fahrni, Jose F.; Vargas, Colomban De; Bowser, Samuel S. (November 1999). "Molecular Evidence That Reticulomyxa Filosa Is A Freshwater Naked Foraminifer". The Journal of Eukaryotic Microbiology. 46 (6): 612–617. doi:10.1111/j.1550-7408.1999.tb05137.x. ISSN 1066-5234. PMID 10568034. S2CID 36497475.
  41. ^ Favulina hexagona European Geosciences Union, 9 November 2020.
  42. ^ Foraminifera: History of Study, University College London. Retrieved: 18 November 2019.
  43. ^ a b Leadbeater BS, Thomsen H (2000). "Order Choanoflagellida". An Illustrated Guide to the Protozoa, Second Edition. Lawrence: Society of Protozoologists. 451: 14–38.
  44. ^ Leadbeater BS, Kelly M (2001). "Evolution of animals choanoflagellates and sponges". Water and Atmosphere Online. 9 (2): 9–11.
  45. ^ Drewes, Charlie. "Discovering Devonian Microfossils". Iowa State University. Retrieved 4 March 2017.
  46. ^ Dodd, Matthew S.; Papineau, Dominic; Grenne, Tor; slack, John F.; Rittner, Martin; Pirajno, Franco; O'Neil, Jonathan; Little, Crispin T. S. (2 March 2017). "Evidence for early life in Earth's oldest hydrothermal vent precipitates" (PDF). Nature. 543 (7643): 60–64. Bibcode:2017Natur.543...60D. doi:10.1038/nature21377. PMID 28252057.
  47. ^ Zimmer, Carl (1 March 2017). "Scientists Say Canadian Bacteria Fossils May Be Earth's Oldest". The New York Times. Retrieved 2 March 2017.
  48. ^ Ghosh, Pallab (1 March 2017). "Earliest evidence of life on Earth 'found". BBC News. Retrieved 2 March 2017.
  49. ^ Dunham, Will (1 March 2017). "Canadian bacteria-like fossils called oldest evidence of life". Reuters. Retrieved 1 March 2017.
  50. ^ Staff (20 August 2018). "A timescale for the origin and evolution of all of life on Earth". Phys.org. Retrieved 20 August 2018.
  51. ^ Betts, Holly C.; Putick, Mark N.; Clark, James W.; Williams, Tom A.; Donoghue, Philip C.J.; Pisani, Davide (20 August 2018). "Integrated genomic and fossil evidence illuminates life's early evolution and eukaryote origin". Nature. 2 (10): 1556–1562. doi:10.1038/s41559-018-0644-x. PMC 6152910. PMID 30127539.

Further references edit

  • Xu, K., Hutchins, D. and Gao, K. (2018) "Coccolith arrangement follows Eulerian mathematics in the coccolithophore Emiliania huxleyi". PeerJ, 6: e4608. doi:10.1126/science.aaa7378.
  • Protistan Skeletons: A Geologic History of Evolution and Constraint

protist, shell, many, protists, have, protective, shells, tests, usually, made, from, silica, glass, calcium, carbonate, chalk, protists, diverse, group, eukaryote, organisms, that, plants, animals, fungi, they, typically, microscopic, unicellular, organisms, . Many protists have protective shells or tests 2 usually made from silica glass or calcium carbonate chalk Protists are a diverse group of eukaryote organisms that are not plants animals or fungi They are typically microscopic unicellular organisms that live in water or moist environments Coccolithophore shellsSize comparison between the relatively large coccolithophore Scyphosphaera apsteinii and the relatively small but ubiquitous coccolithophore Emiliania huxleyi 1 Protists shells are often tough mineralised forms that resist degradation and can survive the death of the protist as a microfossil Although protists are typically very small they are ubiquitous Their numbers are such that their shells play a huge part in the formation of ocean sediments and in the global cycling of elements and nutrients The role of protist shells depends on the type of protist Protists such as diatoms and radiolaria have intricate glass like shells made of silica that are hard and protective and serve as a barrier to prevent water loss The shells have small pores that allow for gas exchange and nutrient uptake Coccolithophores and foraminifera also have hard protective shells but the shells are made of calcium carbonate These shells can help with buoyancy allowing the organisms to float in the water column and move around more easily In addition to protection and support protist shells also serve scientists as a means of identification By examining the characteristics of the shells different species of protists can be identified and their ecology and evolution can be studied Contents 1 Protists 2 Silicon based shells 2 1 Diatoms 2 2 Radiolarians 3 Calcium based shells 3 1 Coccolithophores 3 2 Foraminiferans 4 Other shells 5 Microfossils and sediments 6 See also 7 References 8 Further referencesProtists editCellular life likely originated as single celled prokaryotes including modern bacteria and archaea and later evolved into more complex eukaryotes Eukaryotes include organisms such as plants animals fungi and protists Protists are usually single celled and microscopic They can be heterotrophic meaning they obtain nutrients by consuming other organisms or autotrophic meaning they produce their own food through photosynthesis or chemosynthesis or mixotrophic meaning they produce their own food through a mixture of those methods The term protist came into use historically to refer to a group of biologically similar organisms however modern research has shown it to be a paraphyletic group that does not contain all descendants of a common ancestor As such it does not constitute a clade and is not currently in formal scientific use Nonetheless the term continues to be used informally to refer to those eukaryotes that cannot be classified as plants fungi or animals Most protists are too small to be seen with the naked eye They are highly diverse organisms currently organised into 18 phyla but are not easy to classify 3 4 Studies have shown high protist diversity exists in oceans deep sea vents and river sediments suggesting large numbers of eukaryotic microbial communities have yet to be discovered 5 6 As eukaryotes protists possess within their cell at least one nucleus as well as organelles such as mitochondria and Golgi bodies Many protists are asexual but can reproduce rapidly through mitosis or by fragmentation others including foraminifera may reproduce either sexually or asexually 7 In contrast to the cells of bacteria and archaea the cells of protists and other eukaryotes are highly organised Plants animals and fungi are usually multi celled and are typically macroscopic Most protists are single celled and microscopic but there are exceptions and some marine protists are neither single celled nor microscopic such as seaweed Silicon based shells edit nbsp A diatom enclosed in a silica cell wall See also Biogenic silica Although silicon is readily available in the form of silicates very few organisms use it directly Diatoms radiolaria and siliceous sponges use biogenic silica as a structural material for their skeletons In more advanced plants the silica phytoliths opal phytoliths are rigid microscopic bodies occurring in the cell some plants including rice need silica for their growth 8 9 10 Silica has been shown to improve plant cell wall strength and structural integrity in some plants 11 Diatoms edit Main article diatom frustule See also diatomaceous earth Diatoms form a disputed phylum containing about 100 000 recognised species of mainly unicellular algae Diatoms generate about 20 per cent of the oxygen produced on the planet each year 12 take in over 6 7 billion metric tons of silicon each year from the waters in which they live 13 and contribute nearly half of the organic material found in the oceans Diatoms are enclosed in protective silica glass shells called frustules The beautifully engineered and intricate structure of many of these frustules is such that they are often referred to as jewels of the sea 14 Each frustule is made from two interlocking parts covered with tiny holes through which the diatom exchanges nutrients and wastes 15 The frustules of dead diatoms drift to the ocean floor where over millions of years they can build up as much as half a mile deep 16 Diatoms uses silicon in the biogenic silica BSiO2 form 17 which is taken up by the silicon transport protein to be predominantly used in constructing these protective cell wall structures 18 Silicon enters the ocean in a dissolved form such as silicic acid or silicate 19 Since diatoms are one of the main users of these forms of silicon they contribute greatly to the concentration of silicon throughout the ocean Silicon forms a nutrient like profile in the ocean due to the diatom productivity in shallow depths which means there is less concentration of silicon in the upper ocean and more concentration of silicon in the deep ocean 19 Diatom productivity in the upper ocean contribute to the amount of silicon exported to the lower ocean 20 When diatom cells are lysed in the upper ocean their nutrients like iron zinc and silicon are brought to the lower ocean through a process called marine snow Marine snow involves the downward transfer of particulate organic matter by vertical mixing of dissolved organic matter 21 Availability of silicon appears crucial for diatom productivity and as long as silicic acid is available for diatoms to utilize the diatoms contribute other important nutrient concentrations in the deep ocean 22 In coastal zones diatoms serve as the major phytoplanktonic organisms and greatly contribute to biogenic silica production In the open ocean however diatoms have a reduced role in global annual silica production Diatoms in North Atlantic and North Pacific subtropical gyres contribute only about 6 of global annual marine silica production while the Southern Ocean produces about one third of the global marine biogenic silica 23 The Southern Ocean is referred to as having a biogeochemical divide since only minuscule amounts of silicon is transported out of this region 24 Diatom shapes nbsp nbsp Drawings by Haeckel 1904 nbsp Diatoms are one of the most common types of phytoplankton nbsp Their protective shells frustles are made of silicon nbsp nbsp They come in many shapes and sizes Diatoms nbsp Centric nbsp PennateDiatoms have a silica shell frustule with radial centric or bilateral pennate symmetry nbsp Silicified frustule of a pennate diatom with two overlapping halves nbsp Guinardia delicatula a diatom responsible for algal blooms in the North Sea and the English Channel 25 nbsp Fossil diatom nbsp There are over 100 000 species of diatoms which account for 50 of the ocean s primary production nbsp Different diatom frustule shapes and sizes nbsp Structure of a centric diatom frustule 26 Diatoms nbsp Diatoms major components of marine plankton have silica skeletons called frustules The microscopic structures of diatoms help them manipulate light leading to hopes they could be used in new technologies for light detection computing or robotics 27 nbsp SEM images of pores in diatom frustules 28 Diatom frustules have been accumulating for over 100 million years leaving rich deposits of nano and microstructured silicon oxide in the form of diatomaceous earth around the globe The evolutionary causes for the generation of nano and microstructured silica by photosynthetic algae are not yet clear However in 2018 it was shown that absorption of ultraviolet light by nanostructured silica protects the DNA in the algal cells and this may be an evolutionary cause for the formation of the glass cages 28 29 nbsp Triparma laevis and a drawing of its silicate shell scale bar 1 mm nbsp Exploded drawing of the shell D dorsal plate G girdle plate S shield plate and V ventral plate Triparma laevis belongs to the Bolidophyceae a sister taxon to the diatoms 30 31 External videos nbsp Diatoms Tiny factories you can see from space nbsp How diatoms build their beautiful shells Journey to the Microcosmos Radiolarians edit Radiolarian shapes nbsp nbsp Drawings by Haeckel 1904 Radiolarians are unicellular predatory protists encased in elaborate globular shells usually made of silica and pierced with holes Their name comes from the Latin for radius They catch prey by extending parts of their body through the holes As with the silica frustules of diatoms radiolarian shells can sink to the ocean floor when radiolarians die and become preserved as part of the ocean sediment These remains as microfossils provide valuable information about past oceanic conditions 32 nbsp Like diatoms radiolarians come in many shapes nbsp Also like diatoms radiolarian shells are usually made of silicate nbsp However acantharian radiolarians have shells made from strontium sulfate crystals nbsp An animation of the diversity of radiolarian shells 33 nbsp Cutaway schematic diagram of a spherical radiolarian shell nbsp Cladococcus abietinus Fossil radiolarian nbsp X ray microtomography of Triplococcus acanthicus This is a microfossil from the Middle Ordovician with four nested spheres The innermost sphere is highlighted red Each segment is shown at the same scale 34 Turing and radiolarian morphology nbsp Shell of a spherical radiolarian nbsp Shell micrographsComputer simulations of Turing patterns on a sphere closely replicate some radiolarian shell patterns 35 External videos nbsp Radiolarian geometry nbsp Ernst Haeckel s radiolarian engravingsCalcium based shells editSee also Marine biogenic calcification Coccolithophores edit Further information coccoliths Coccolithophores are minute unicellular photosynthetic protists with two flagella for locomotion Most of them are protected by a shell called a coccosphere Coccospheres are covered with ornate circular plates or scales called coccoliths The coccoliths are made from calcium carbonate The term coccolithophore derives from the Greek for a seed carrying stone referring to their small size and the coccolith stones they carry Under the right conditions they bloom like other phytoplankton and can turn the ocean milky white 36 nbsp nbsp Coccolithophores named after the BBC documentary series The Blue Planet nbsp The coccolithophore Emiliania huxleyi Coccolithophores nbsp Have plates called coccoliths nbsp Extinct fossilCoccolithophores build calcite skeletons important to the marine carbon cycle 37 There are benefits for protists that carry protective shells The diagram on the left below shows some benefits coccolithophore get from carrying coccoliths In the diagram A represents accelerated photosynthesis including carbon concentrating mechanisms CCM and enhanced light uptake via scattering of scarce photons for deep dwelling species B represents protection from photodamage including sunshade protection from ultraviolet light UV and photosynthetic active radiation PAR and energy dissipation under high light conditions C represents armour protection includes protection against viral bacterial infections and grazing by selective and nonselective grazers 38 Benefits of having shells nbsp Benefits in coccolithophore calcification 38 see text above Costs of having shells nbsp Energetic costs in coccolithophore calcification 38 There are also costs for protists that carry protective shells The diagram on the right above shows some of the energetic costs coccolithophore incur from carrying coccoliths In the diagram the energetic costs are reported in percentage of total photosynthetic budget A represents transport processes include the transport into the cell from the surrounding seawater of primary calcification substrates Ca2 and HCO3 black arrows and the removal of the end product H from the cell gray arrow The transport of Ca2 through the cytoplasm to the coccolith vesicle CV is the dominant cost associated with calcification B represents metabolic processes include the synthesis of coccolith associated polysaccharides CAPs gray rectangles by the Golgi complex white rectangles that regulate the nucleation and geometry of CaCO3 crystals The completed coccolith gray plate is a complex structure of intricately arranged CAPs and CaCO3 crystals C Mechanical and structural processes account for the secretion of the completed coccoliths that are transported from their original position adjacent to the nucleus to the cell periphery where they are transferred to the surface of the cell 38 Foraminiferans edit Main article foraminifera test Foraminiferan shapes nbsp nbsp Drawings by Haeckel 1904 Like radiolarians foraminiferans forams for short are single celled predatory protists also protected with shells that have holes in them Their name comes from the Latin for hole bearers Their shells often called tests may be single chambered or multi chambered multi chambered forams add more chambers as they grow The most famous of these are made of calcite but tests may also be made of aragonite agglutinated sediment particles chiton or rarely of silica Most forams are benthic but about 40 living species are planktic 39 They are widely researched with well established fossil records which allow scientists to infer a lot about past environments and climates 32 Some foraminifera lack tests altogether 40 Foraminiferans nbsp Empty Foraminiferan test showing multiple chambers and pores nbsp and in life showing pseudopodia streaming from poresForaminiferans are important unicellular zooplankton protists often with calcite tests External videos nbsp foraminiferans nbsp Foraminiferal networks and growth nbsp Benthic foraminifera Favulina hexagona together with nanofossils enclosed inside the shell hexagons 41 nbsp section showing chambers of a spiral foram nbsp Live Ammonia tepida streaming granular ectoplasm for catching food nbsp Group of planktonic forams nbsp Fossil nummulitid forams of various sizes from the Eocene nbsp The Egyptian pyramids were constructed from limestone that contained nummulites 42 Other shells edit nbsp Testate amoeba The cell body of many choanoflagellates is surrounded by a distinguishing extracellular matrix or periplast These cell coverings vary greatly in structure and composition and are used by taxonomists for classification purposes Many choanoflagellates build complex basket shaped houses called lorica from several silica strips cemented together 43 The functional significance of the periplast is unknown but in sessile organisms it is thought to aid attachment to the substrate In planktonic organisms there is speculation that the periplast increases drag thereby counteracting the force generated by the flagellum and increasing feeding efficiency 43 44 External videos nbsp Testate amoebas blobby modest shell dwellers Journey to the Microcosmos nbsp ChoanoflagellateMicrofossils and sediments edit nbsp Diatomaceous earth is a soft siliceous sedimentary rock made up of microfossils in the form of the frustules shells of single cell diatoms This sample consists of a mixture of centric radially symmetric and pennate bilaterally symmetric diatoms Click 3 times to fully enlarge Main article Protists in the fossil record See also Microfossil Pelagic sediment Diatomaceous earth and Siliceous ooze The shells or skeletons of many protists survive over geological time scales as microfossils Microfossils are fossils that are generally between 0 001mm and 1 mm in size 45 the study of which requires the use of light or electron microscopy Fossils which can be studied by the naked eye or low powered magnification such as a hand lens are referred to as macrofossils Microfossils are a common feature of the geological record from the Precambrian to the Holocene They are most common in marine sediments but also occur in brackish water fresh water and terrestrial sedimentary deposits While every kingdom of life is represented in the microfossil record the most abundant forms are protist skeletons or cysts from the Chrysophyta Pyrrhophyta Sarcodina acritarchs and chitinozoans together with pollen and spores from the vascular plants In 2017 fossilized microorganisms or microfossils were discovered in hydrothermal vent precipitates in the Nuvvuagittuq Belt that may be as old as 4 28 billion years old the oldest record of life on Earth suggesting an almost instantaneous emergence of life in a geological time scale sense after ocean formation 4 41 billion years ago and not long after the formation of the Earth 4 54 billion years ago 46 47 48 49 Nonetheless life may have started even earlier at nearly 4 5 billion years ago as claimed by some researchers 50 51 See also editCytoskeleton Particulate inorganic matterReferences edit Gafar N A Eyre B D and Schulz K G 2019 A comparison of species specific sensitivities to changing light and carbonate chemistry in calcifying marine phytoplankton Scientific Reports 9 1 1 12 doi 10 1038 s41598 019 38661 0 nbsp Material was copied from this source which is available under a Creative Commons Attribution 4 0 International License Groups of Protists Boundless Biology courses lumenlearning com Retrieved 16 February 2021 Cavalier Smith T December 1993 Kingdom protozoa and its 18 phyla Microbiological Reviews 57 4 953 94 doi 10 1128 mmbr 57 4 953 994 1993 PMC 372943 PMID 8302218 Corliss JO 1992 Should there be a separate code of nomenclature for the protists BioSystems 28 1 3 1 14 doi 10 1016 0303 2647 92 90003 H PMID 1292654 Slapeta J Moreira D Lopez Garcia P 2005 The extent of protist diversity insights from molecular ecology of freshwater eukaryotes Proceedings of the Royal Society B Biological Sciences 272 1576 2073 81 doi 10 1098 rspb 2005 3195 PMC 1559898 PMID 16191619 Moreira D Lopez Garcia P 2002 The molecular ecology of microbial eukaryotes unveils a hidden world PDF Trends in Microbiology 10 1 31 8 doi 10 1016 S0966 842X 01 02257 0 PMID 11755083 Foraminifera notes for a short course organized by M A Buzas and B K Sen Gupta prepared for the short course on foraminifera sponsored by the Paleontological Society held at New Orleans Louisiana October 17 1982 Thomas W Broadhead Paleontological Society Knoxville Tenn University of Tennessee Dept of Geological Sciences 1982 ISBN 0 910249 05 9 OCLC 9276403 a href Template Cite book html title Template Cite book cite book a CS1 maint others link Rahman Atta ur 2008 Silicon Studies in Natural Products Chemistry Vol 35 p 856 ISBN 978 0 444 53181 0 Exley C 1998 Silicon in life A bioinorganic solution to bioorganic essentiality Journal of Inorganic Biochemistry 69 3 139 144 doi 10 1016 S0162 0134 97 10010 1 Epstein Emanuel 1999 SILICON Annual Review of Plant Physiology and Plant Molecular Biology 50 641 664 doi 10 1146 annurev arplant 50 1 641 PMID 15012222 Kim Sang Gyu Kim Ki Woo Park Eun Woo Choi Doil 2002 Silicon Induced Cell Wall Fortification of Rice Leaves A Possible Cellular Mechanism of Enhanced Host Resistance to Blast Phytopathology 92 10 1095 103 doi 10 1094 PHYTO 2002 92 10 1095 PMID 18944220 The Air You re Breathing A Diatom Made That Treguer P Nelson D M Van Bennekom A J Demaster D J Leynaert A Queguiner B 1995 The Silica Balance in the World Ocean A Reestimate Science 268 5209 375 9 Bibcode 1995Sci 268 375T doi 10 1126 science 268 5209 375 PMID 17746543 S2CID 5672525 Ireland T Engineering with algae Biologist 63 5 10 Wassilieff Maggy 2006 Plankton Plant plankton Te Ara the Encyclopedia of New Zealand Accessed 2 November 2019 King s College London Lake Megachad www kcl ac uk Retrieved 5 May 2018 Bidle Kay D Manganelli Maura Azam Farooq 6 December 2002 Regulation of Oceanic Silicon and Carbon Preservation by Temperature Control on Bacteria Science 298 5600 1980 1984 Bibcode 2002Sci 298 1980B doi 10 1126 science 1076076 ISSN 0036 8075 PMID 12471255 S2CID 216994 Durkin Colleen A Koester Julie A Bender Sara J Armbrust E Virginia 2016 The evolution of silicon transporters in diatoms Journal of Phycology 52 5 716 731 doi 10 1111 jpy 12441 ISSN 1529 8817 PMC 5129515 PMID 27335204 a b Dugdale R C Wilkerson F P 30 December 2001 Sources and fates of silicon in the ocean the role of diatoms in the climate and glacial cycles Scientia Marina 65 S2 141 152 doi 10 3989 scimar 2001 65s2141 ISSN 1886 8134 Baines Stephen B Twining Benjamin S Brzezinski Mark A Krause Jeffrey W Vogt Stefan Assael Dylan McDaniel Hannah December 2012 Significant silicon accumulation by marine picocyanobacteria Nature Geoscience 5 12 886 891 Bibcode 2012NatGe 5 886B doi 10 1038 ngeo1641 ISSN 1752 0908 Turner Jefferson T January 2015 Zooplankton fecal pellets marine snow phytodetritus and the ocean s biological pump Progress in Oceanography 130 205 248 Bibcode 2015PrOce 130 205T doi 10 1016 j pocean 2014 08 005 ISSN 0079 6611 Yool Andrew Tyrrell Toby 2003 Role of diatoms in regulating the ocean s silicon cycle Global Biogeochemical Cycles 17 4 n a Bibcode 2003GBioC 17 1103Y doi 10 1029 2002GB002018 ISSN 1944 9224 S2CID 16849373 Treguer Paul J De La Rocha Christina L 3 January 2013 The World Ocean Silica Cycle Annual Review of Marine Science 5 1 477 501 doi 10 1146 annurev marine 121211 172346 PMID 22809182 Marinov I Gnanadesikan A Toggweiler J R Sarmiento J L June 2006 The Southern Ocean biogeochemical divide Nature 441 7096 964 967 Bibcode 2006Natur 441 964M doi 10 1038 nature04883 PMID 16791191 S2CID 4428683 Arsenieff L Simon N Rigaut Jalabert F Le Gall F Chaffron S Corre E Com E Bigeard E Baudoux A C 2018 First Viruses Infecting the Marine Diatom Guinardia delicatula Frontiers in Microbiology 9 3235 doi 10 3389 fmicb 2018 03235 PMC 6334475 PMID 30687251 Zhang D Wang Y Cai J Pan J Jiang X Jiang Y 2012 Bio manufacturing technology based on diatom micro and nanostructure Chinese Science Bulletin 57 30 3836 3849 Bibcode 2012ChSBu 57 3836Z doi 10 1007 s11434 012 5410 x Biodegradable glitter and pollution eating microalgae the new materials inspired by nature Horizon 28 May 2020 a b Aguirre L E Ouyang L Elfwing A Hedblom M Wulff A and Inganas O 2018 Diatom frustules protect DNA from ultraviolet light Scientific reports 8 1 1 6 doi 10 1038 s41598 018 21810 2 nbsp Material was copied from this source which is available under a Creative Commons Attribution 4 0 International License De Tommasi E Congestri R Dardano P De Luca A C Manago S Rea I and De Stefano M 2018 UV shielding and wavelength conversion by centric diatom nanopatterned frustules Scientific Reports 8 1 1 14 doi 10 1038 s41598 018 34651 w nbsp Material was copied from this source which is available under a Creative Commons Attribution 4 0 International License Booth B C and Marchant H J 1987 Parmales a new order of marine chrysophytes with descriptions of three new genera and seven new species Journal of Phycology 23 245 260 doi 10 1111 j 1529 8817 1987 tb04132 x Kuwata A Yamada K Ichinomiya M Yoshikawa S Tragin M Vaulot D and Lopes dos Santos A 2018 Bolidophyceae a sister picoplanktonic group of diatoms a review Frontiers in Marine Science 5 370 doi 10 3389 fmars 2018 00370 nbsp Material was copied from this source which is available under a Creative Commons Attribution 4 0 International License a b Wassilieff Maggy 2006 Plankton Animal plankton Te Ara the Encyclopedia of New Zealand Accessed 2 November 2019 Kachovich Sarah 2018 Minds over Methods Linking microfossils to tectonics Blog of the Tectonics and Structural Geology Division of the European Geosciences Union Kachovich S Sheng J and Aitchison J C 2019 Adding a new dimension to investigations of early radiolarian evolution Scientific reports 9 1 pp 1 10 doi 10 1038 s41598 019 42771 0 nbsp Material was copied from this source which is available under a Creative Commons Attribution 4 0 International License Varea C Aragon J L Barrio R A 1999 Turing patterns on a sphere Physical Review E 60 4 4588 4592 Bibcode 1999PhRvE 60 4588V doi 10 1103 PhysRevE 60 4588 PMID 11970318 Wassilieff Maggy 2006 A coccolithophore Te Ara the Encyclopedia of New Zealand Accessed 2 November 2019 Rost B and Riebesell U 2004 Coccolithophores and the biological pump responses to environmental changes In Coccolithophores From Molecular Processes to Global Impact pages 99 125 Springer ISBN 9783662062784 a b c d Monteiro F M Bach L T Brownlee C Bown P Rickaby R E Poulton A J Tyrrell T Beaufort L Dutkiewicz S Gibbs S and Gutowska M A 2016 Why marine phytoplankton calcify Science Advances 2 7 e1501822 doi 10 1126 sciadv 1501822 nbsp Material was copied from this source which is available under a Creative Commons Attribution 4 0 International License Hemleben C Anderson O R Spindler M 1989 Modern Planktonic Foraminifera Springer Verlag ISBN 978 3 540 96815 3 Pawlowski Jan Bolivar Ignacio Fahrni Jose F Vargas Colomban De Bowser Samuel S November 1999 Molecular Evidence That Reticulomyxa Filosa Is A Freshwater Naked Foraminifer The Journal of Eukaryotic Microbiology 46 6 612 617 doi 10 1111 j 1550 7408 1999 tb05137 x ISSN 1066 5234 PMID 10568034 S2CID 36497475 Favulina hexagona European Geosciences Union 9 November 2020 Foraminifera History of Study University College London Retrieved 18 November 2019 a b Leadbeater BS Thomsen H 2000 Order Choanoflagellida An Illustrated Guide to the Protozoa Second Edition Lawrence Society of Protozoologists 451 14 38 Leadbeater BS Kelly M 2001 Evolution of animals choanoflagellates and sponges Water and Atmosphere Online 9 2 9 11 Drewes Charlie Discovering Devonian Microfossils Iowa State University Retrieved 4 March 2017 Dodd Matthew S Papineau Dominic Grenne Tor slack John F Rittner Martin Pirajno Franco O Neil Jonathan Little Crispin T S 2 March 2017 Evidence for early life in Earth s oldest hydrothermal vent precipitates PDF Nature 543 7643 60 64 Bibcode 2017Natur 543 60D doi 10 1038 nature21377 PMID 28252057 Zimmer Carl 1 March 2017 Scientists Say Canadian Bacteria Fossils May Be Earth s Oldest The New York Times Retrieved 2 March 2017 Ghosh Pallab 1 March 2017 Earliest evidence of life on Earth found BBC News Retrieved 2 March 2017 Dunham Will 1 March 2017 Canadian bacteria like fossils called oldest evidence of life Reuters Retrieved 1 March 2017 Staff 20 August 2018 A timescale for the origin and evolution of all of life on Earth Phys org Retrieved 20 August 2018 Betts Holly C Putick Mark N Clark James W Williams Tom A Donoghue Philip C J Pisani Davide 20 August 2018 Integrated genomic and fossil evidence illuminates life s early evolution and eukaryote origin Nature 2 10 1556 1562 doi 10 1038 s41559 018 0644 x PMC 6152910 PMID 30127539 Further references editXu K Hutchins D and Gao K 2018 Coccolith arrangement follows Eulerian mathematics in the coccolithophore Emiliania huxleyi PeerJ 6 e4608 doi 10 1126 science aaa7378 Protistan Skeletons A Geologic History of Evolution and Constraint Retrieved from https en wikipedia org w index php title Protist shell amp oldid 1216249738, wikipedia, wiki, book, books, library,

article

, read, download, free, free download, mp3, video, mp4, 3gp, jpg, jpeg, gif, png, picture, music, song, movie, book, game, games.